| common in clinvar |
| Is a | genotype |
| of | rs267608058 |
| Gene | MSH6 |
| Chromosome | 2 |
| Position | 47,800,133 |
| Merged from | Rs587782275 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;TCAG) | 6 | Lynch syndrome, pathogenic mutation |
| (CAGT;CAGT) | 0 | common in clinvar |
| (TCAG;TCAG) | 0 | common in clinvar |
